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Efficacy and Safety Evaluation of TDF-based Regimen in Thai HIV-infected Children
This study will assess the safety and efficacy of generic TDF from Governmental Pharmaceutical Organization (GPO) in HIV-infected children
TDF is a nucleotide reverse transcriptase inhibitor (NRTI) which can be taken only once per day and continues to have good efficacy even in patients who have resistance to other NNRTI in the absence of K65R mutation. TDF is a choice for patients with NRTI resistance, or those that require once-daily regimen to improve adherence. Currently, TDF has not been approved by the US FDA for children less than 18 years, but pediatricians has been using TDF in children who have treatment failure because of limitation of a more appropriate pediatric ARV. The Thai national guideline for pediatric 2009 recommend the use of TDF in children who have failed the first line therapy with multi-NRTI mutation and are more than 30 kilograms or have tanner stage 4 or more. However, the problem is that there is no pediatric TDF formulation. The available preparation of 300 mg tear drop tablet, if cut in half, may increase dosing errors, more or less by 18-37%. This will affect the blood level and/or toxicities. Therefore, the Thai Governmental Pharmaceutical Organization (GPO) has produced a generic TDF formulation that can be used in HIV-infected children. This study will assess the safety and efficacy information in children using this generic pediatric TDF formulation.
Age
8 - 18 years
Sex
ALL
Healthy Volunteers
No
HIV-NAT
Bangkok, Thailand
King Chulalongkorn Hospital, Chulalongkorn University
Bangkok, Thailand
Start Date
December 1, 2010
Primary Completion Date
August 1, 2013
Completion Date
August 1, 2013
Last Updated
July 17, 2020
36
ACTUAL participants
tenofovir (TDF)
DRUG
Lead Sponsor
The HIV Netherlands Australia Thailand Research Collaboration
Collaborators
Data Source & Attribution
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